raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:75508

Angioosteohypotrophic syndrome

inactive · moved to ORPHA:217008Segmental venous malformation

Synonyms: Phlebectatic osteohypoplastic angiodysplasia · Servelle-Martorell syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Segmental venous malformation

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAngioosteohypotrophic syndromePhlebectatic osteohypoplastic angiodysplasia · Servelle-Martorell syndrome
frSyndrome angio-ostéo-hypotrophiqueSyndrome de Servelle-Martorell
deAngio-osteo-hypotrophisches SyndromAngiodysplasie, osteohypoplastische phlebektatische · Servelle-Martorell-Syndrom
esSíndrome angio-osteo-hipotróficoSíndrome de Servelle-Martorell
itSindrome angio-osteoipotroficaAngiodisplasia osteo-ipoplasica flebectasica · Sindrome di Servelle-Martorell
nlAngio-osteohypotrofisch syndroomFlebectatische osteohypoplastische angiodysplasie · Syndroom van Servelle-Martorell
ptSíndrome angio-osteo-hipotróficoSíndrome de Servelle-Martorell
plZespół naczyniowo-osteohipotroficznyZespół Servelle'a i Martorella
csAngioosteohypotrofický syndromFlebektatická osteohypoplastická angiodysplázie · Servellův-Martorellův syndrom · Servelle-Martorellův syndrom
ukАнгіоостеогіпотрофічний синдромФлебектатична остеогіпопластична ангіодисплазія · Синдром Сервеля-Мартореля
zh血管骨营养不良综合征血管骨营养不良综合征
trAnjiyoosteohipotrofik sendromServelle-Martorell sendromu · Flebektatik osteohipoplastik anjiyodisplazi

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0019156Evalidated
UMLSC4707561Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card